Ring-closing metathesis as a tool for the efficient preparation of chiral spirocyclic ethers from homoallylic alcohols
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Nonanomeric Spiroketals in Natural Products: Structures, Sources, and Synthetic Strategies
2. Selected Synthetic Strategies to Spirocyclics
3. Stereocontrolled oxaspirocyclization of conjugated dienes via palladium catalysis
4. Oxonium ion-initiated pinacolic ring expansion reactions. Application to the enantioselective synthesis of the spirocyclic sesquiterpene ethers dactyloxene-B and -C
5. Syntheses of Theaspirone and Vitispirane via Palladium(II)-Catalyzed Oxaspirocyclization
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1. Stereoselective construction of sterically hindered oxaspirocycles via chiral bidentate directing group-mediated C(sp3)–O bond formation;Chemical Science;2018
2. Optically active tertiary alcohols by biocatalysis;Synthetic Communications;2017-02-03
3. Olefin Ring‐Closing Metathesis;Organic Reactions;2016-02
4. Diversity-oriented approach to natural product inspired pyrano-carbazole derivatives: strategic utilization of hetero-Diels–Alder reaction, Fischer indolization and the Suzuki–Miyaura cross-coupling reaction;Tetrahedron;2015-11
5. A simple approach to bis-spirocycles and spiroindole derivatives via green methods such as Fischer indolization, ring-closing metathesis, and Suzuki--Miyaura cross-coupling;TURKISH JOURNAL OF CHEMISTRY;2015
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